Ceramill Zolid HT+ white

FDA 510(k) K171876 · Amann Girrbach AG

Substantially Equivalent

510(k) numberK171876

Submission

Device name
Ceramill Zolid HT+ white
Applicant
Amann Girrbach AG
Koblach, AT
Received
June 23, 2017
Decision date
September 20, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EIH – Powder, Porcelain
Device class
Class II (moderate risk)
Regulation
21 CFR 872.6660
Specialty
Dental

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Questions and answers

When was Ceramill Zolid HT+ white cleared by the FDA?

Ceramill Zolid HT+ white (K171876) received a 510(k) decision of Substantially Equivalent on September 20, 2017, 89 days after the submission was received.

What is the product code of K171876?

The FDA product code is EIH – Powder, Porcelain, a Class II (moderate risk) device regulated under 21 CFR 872.6660.